mafdr Search Results


mafdr.m function  (MathWorks Inc)
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mafdr function  (MathWorks Inc)
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MathWorks Inc mafdr function
Mafdr Function, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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function mafdr  (MathWorks Inc)
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MathWorks Inc function mafdr
Function Mafdr, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mafdr function in matlab r2012a  (MathWorks Inc)
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MathWorks Inc mafdr function in matlab r2012a
Mafdr Function In Matlab R2012a, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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matlab function 'mafdr  (MathWorks Inc)
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MathWorks Inc matlab function 'mafdr
( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
Matlab Function 'mafdr, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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matlab function 'mafdr - by Bioz Stars, 2026-03
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matlab function mafdr.m  (MathWorks Inc)
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MathWorks Inc matlab function mafdr.m
( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
Matlab Function Mafdr.M, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mafdr function version 7.5.0  (MathWorks Inc)
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MathWorks Inc mafdr function version 7.5.0
( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
Mafdr Function Version 7.5.0, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mafdr function version 7.5.0 - by Bioz Stars, 2026-03
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mafdr  (MathWorks Inc)
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MathWorks Inc mafdr
( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
Mafdr, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mafdr/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
mafdr - by Bioz Stars, 2026-03
90/100 stars
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function mafdr.m  (MathWorks Inc)
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MathWorks Inc function mafdr.m
( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
Function Mafdr.M, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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Image Search Results


( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null hypotheses that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.

Journal: eLife

Article Title: Hierarchy between forelimb premotor and primary motor cortices and its manifestation in their firing patterns

doi: 10.7554/eLife.103069

Figure Lengend Snippet: ( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null hypotheses that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.

Article Snippet: From distributions of p-values calculated as described below for each metric, we estimated the fraction of false null hypotheses as one minus an estimate of the a prior i fraction of true null hypotheses ( ) (MATLAB function ‘mafdr’).

Techniques: Modification, Control